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TIP OFF FORCEPS

K854541 Class I Traditional
Decision Date
1985-12-17
Sponsor / Applicant
Keller Instruments, Inc.

Technical Specification

510(k) Submission ID K854541
Product Code GEN
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1985-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TIP OFF FORCEPS received FDA 510(k) clearance under submission number K854541, sponsored by Keller Instruments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1985-12-17.

Classification & Regulation

This clearance is catalogued under FDA product code GEN and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.